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在资源有限国家接受治疗并经国际慢性粒细胞白血病基金会(iCMLf)专家讨论的患者病例 - 病例1:一名出现阴茎异常勃起和视力丧失的男孩。

Cases of Patients Treated in Countries With Limited Resources and Discussed by Experts of the International CML Foundation (iCMLf)-Case No. 1: A Boy Presenting With Priapism and Loss of Vision.

作者信息

Moulik Nirmalya Roy, Harriss-Buchan Arlene, Saglio Guiseppe, Evans Nicola, Suttorp Meinolf

机构信息

Tata Memorial Hospital Homi Bhabha National Institute, Mumbai, India.

International CML Foundation, Bexhill-on-Sea, UK.

出版信息

Case Rep Oncol Med. 2024 Jul 29;2024:5534445. doi: 10.1155/2024/5534445. eCollection 2024.

Abstract

Pediatric chronic myeloid leukemia (pCML) is a rare malignancy accounting for only 2%-3% of all childhood leukemias. Due to this rarity, familiarity with pCML is limited among most pediatric practitioners, including even pediatric hemato-oncologists. In low- and middle-income countries (LMICs), limited financial resources and limited data specific to pCML represent obstacles that healthcare providers must face in diagnosing and treating this rare condition in children. The International CML Foundation (iCMLf) is improving outcomes for people with CML in these countries where resources, diagnostics, and access to medicines may be limited (https://www.cml-foundation.org/lmic-programs.html). Virtual meetings with the purpose of teaching participating pediatricians from LMICs of defined geographical regions were organised by the iCMLf in 2023. At a virtual meeting of the South Asia region, the case of a 14-year-old Indian boy was presented diagnosed with CML in a chronic phase complicated by priapism and loss of vision in his left eye due to hyperleukocytosis. Key aspects of this case are discussed in-depth from the perspective of (i) a pediatric hemato-oncologist practicing in a high-income country, (ii) a pediatric hemato-oncologist practicing in a LMIC, (iii) an adult CML hematologist, and (iv) from the iCMLf in improving the care of children with CML worldwide. Thus by discussing a multifaceted complicated case of pCML in written form as well as pointing to the pediatric module of the iCMLf Knowledge Centre will hopefully contribute to minimize existing knowledge gaps in a rare pediatric malignancy.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/069b/11300043/c80068948050/CRIONM2024-5534445.001.jpg

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